Severe Arterial Forearm Thrombosis in an 11-year-old Girl with Homozygous Antithrombin Deficiency typ IIb Budapest 3 and Mild Factor VII Deficiency Due to Homozygous Polymorphisms in the Factor 7 Gene and Antithrombotic Treatment
Science meets clinical practiceHämostaseologie(2019)
摘要
Background: Inherited antithrombin (AT) type IIb Budapest 3 (AT Bp3) deficiency is a rare disorder affecting the heparin binding site of AT. Homozygosity for ATBp3 deficiency in contrast to a homozygous AT type I deficiency may not be fatal.
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关键词
homozygous antithrombin deficiency typ,mild factor vii deficiency,severe arterial forearm thrombosis,homozygous polymorphisms,year-old
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